Clinical Research Associate

PowerToFly; Lisboa; Híbrido; EUR 35 000 - 52 000; Tempo integral

Resumo da oferta

AbbVie in Amadora, Portugal, is seeking a Clinical Research Associate to join our Clinical Operations team in a hybrid role. In this position, you will contribute to the successful delivery of AbbVie clinical studies by building strong partnerships with investigators and site staff, ensuring high-quality study conduct, and supporting the protection and safety of study participants.

You will work closely with clinical study teams and investigative sites across Phase I-IV studies, gaining exposure

Qualificações

• Bachelor’s degree in a health-related or scientific discipline.
• Minimum of one year in clinical research monitoring.
• Strong planning, organizational and communication skills.
• Ability to manage multiple priorities and collaborate with study teams.

Responsabilidades

• Build partnerships with investigators and site staff aligned with study objectives and regulatory expectations.
• Conduct site qualification, initiation, routine monitoring, and close-out visits for Phase I–IV studies.
• Train site personnel on the protocol, study procedures, safety reporting, and regulatory expectations.
• Oversee site activities, identify risks, and support corrective and preventive actions with stakeholders.
• Ensure timely data submission and reporting, while protecting participant safety.
• Support patient recruitment and retention by understanding patient journey and local site realities.
• Identify and evaluate potential investigators and sites using local knowledge and networks.
• Maintain site and study documentation in inspection-ready state.
• Manage investigator payments and expense reports per contractual obligations.
• Contribute to site engagement strategies with local insights and monitoring outcomes.

Conhecimentos

Planning & Organization

Communication Skills

Interpersonal Skills

Team Collaboration

Formação académica

Bachelor's degree or equivalent in health-related or scientific discipline

Descrição da oferta de emprego

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com.

Job Description

We are looking for a Clinical Research Associate (CRA) to join our Clinical Operations team in Amadora, Portugal, in a hybrid role. In this position, you will contribute to the successful delivery of AbbVie clinical studies by building strong partnerships with investigators and site staff, ensuring high-quality study conduct, and supporting the protection and safety of study participants.

You will work closely with clinical study teams and investigative sites across Phase I-IV studies, gaining exposure to a wide range of clinical research activities in a collaborative and patient-focused environment. This is an excellent opportunity for a motivated clinical research professional to develop their expertise while contributing to the advancement of innovative medicines.

Key Responsibilities

• Build trusted and effective partnerships with investigators and site staff by aligning them with study objectives, protocol requirements, patient treatment principles, and applicable regulatory expectations.
• Conduct site qualification, site initiation, routine on-site and remote monitoring, and study close-out visits for Phase I-IV clinical studies, in accordance with the protocol, monitoring plan, GCP, ICH guidelines, AbbVie SOPs, and applicable regulations.
• Train site personnel on the protocol, study procedures, safety reporting requirements, and relevant regulatory expectations, in collaboration with the clinical study team.
• Oversee site activities, proactively identify risks and compliance issues, and support the implementation and follow-up of corrective and preventive action plans in collaboration with Central Monitoring and relevant stakeholders.
• Ensure the quality and timely submission of data from investigative sites, including appropriate reporting and follow-up of safety events, while supporting the protection and safety of study participants.
• Support patient recruitment and retention activities by applying an understanding of the patient journey, therapeutic area, and local site realities.
• Identify, evaluate, and recommend potential investigators and investigative sites, using local knowledge, professional networks, and internal AbbVie resources as appropriate.
• Maintain site and study documentation in an inspection-ready state and support regulatory inspection readiness at assigned sites.
• Manage investigator payments in line with executed contractual obligations, support the negotiation of investigator and hospital agreements with relevant stakeholders, and complete expense reports in accordance with local requirements and applicable guidelines.
• Contribute to site engagement strategies by gathering local insights, tracking progress, reporting outcomes, and identifying opportunities for continuous improvement.

Qualifications

• Bachelor’s degree or equivalent qualification in a health-related or scientific discipline preferred, such as Medicine, Nursing, Pharmacy, Life Sciences, or a related field.
• Minimum ofone year in clinical research monitoring.
• Strong planning, organizational, communication, and interpersonal skills, with the ability to manage multiple priorities and collaborate effectively with study teams, investigators, and site staff.
• Good analytical and problem-solving skills, with the ability to identify site issues, exercise sound judgment, and support appropriate corrective actions.
• Self-motivated and collaborative, with a strong commitment to quality, compliance, patient safety, ethical conduct, and timely delivery.

Additional Information

AbbVie Culture

At AbbVie, we care deeply about bringing innovative solutions to patients in need. By joining us as a CRA, you'll be at the forefront of our mission, working in a dynamic and supportive environment that encourages growth and collaboration.

• All4OneAbbVie: Foster strong interpersonal relationships and teamwork.
• Decide Smart & Sure: Navigate ambiguity and make informed decisions.
• Agile & Accountable: Communicate a clear and inspiring vision.
• Clear & Courageous: Provide honest and constructive feedback.
• Make Possibilities Real: Efficiently plan and execute tasks while adapting to challenges.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

What AbbVie Has to Offer

Our work can -and does -have a tangible, lasting impact on millions of people. But it's not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.